ENST00000272286.4:c.1630A>G
MANE Select
|
ENSP00000272286.2:p.Ile544Val
|
|
ENST00000272286.2:c.1630A>G
|
ENSP00000272286.2:p.Ile544Val
|
|
NM_022437.2:c.1630A>G
|
NP_071882.1:p.Ile544Val
|
|
XM_005264483.2:c.1627A>G
|
XP_005264540.1:p.Ile543Val
|
|
XM_011533029.1:c.1642A>G
|
XP_011531331.1:p.Ile548Val
|
|
XM_011533030.1:c.1639A>G
|
XP_011531332.1:p.Ile547Val
|
|
XM_011533031.1:c.1414A>G
|
XP_011531333.1:p.Ile472Val
|
|
XR_939707.1:n.2132A>G
|
|
|
NM_001357321.1:c.1627A>G
|
NP_001344250.1:p.Ile543Val
|
|
XM_011533029.2:c.1642A>G
|
XP_011531331.1:p.Ile548Val
|
|
XM_011533030.2:c.1639A>G
|
XP_011531332.1:p.Ile547Val
|
|
XR_001738891.1:n.2146A>G
|
|
|
XR_939707.2:n.2146A>G
|
|
|
NM_022437.3:c.1630A>G
MANE Select
|
NP_071882.1:p.Ile544Val
|
|
NM_001357321.2:c.1627A>G
|
NP_001344250.1:p.Ile543Val
|
|